Full data view for gene GPR98


This database is one of the ”Retinal and hearing impairment genetic variant databases”. NOTE: gene symbol was recently changed from GPR98 to ADGRV1.
Information The variants shown are described using the NM_032119.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/? 84 c.17933A>G r.(?) p.(His5978Arg) Extracellular 1 (5961-5979) Paternal (confirmed) ACMG VUS g.90261308A>G g.90965491A>G - - GPR98_000206 heterozygous; UV3 PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/170 controls +HpyCH4IV;+AflIII; - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 84 c.17933A>G r.(?) p.(His5978Arg) Extracellular 1 (5961-5979) Maternal (confirmed) ACMG VUS g.90261308A>G g.90965491A>G - - GPR98_000206 heterozygous; UV3 PubMed: Besnard 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/170 controls +HpyCH4IV;+AflIII; - - DNA SEQ - - USH2 - PubMed: Besnard 2012 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. - c.17933A>G r.(?) p.(His5978Arg) - Both (homozygous) - pathogenic (recessive) g.90261308A>G g.90965491A>G - - GPR98_000206 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP956 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
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